반응 #742295

ord-e9b5d1c8fa2f4f39b791aafb805c59d5

반응 방정식

CC(C)(C)[Si](C)(C)Cl
tert-Butyldimethylsilyl chloride
OC1CN(C(c2ccccc2)c2ccccc2)C1
1-benzhydrylazetidin-3-ol
c1c[nH]cn1
imidazole
CC(C)(C)[Si](C)(C)OC1CN(C(c2ccccc2)c2ccccc2)C1
product
수율 113.0%
CC(C)(C)[Si](C)(C)OC1CN(C(c2ccccc2)c2ccccc2)C1
(1-Benzhydrylazetidin-3-yl)oxy-tert-butyl-dimethylsilane
수율 113.0%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타at r.t.
  2. 2
    기타The reaction mixture was quenched with water
  3. 3
    workup.ADDITIONpoured onto a phase separator
  4. 4
    기타evaporated

실험 절차

tert-Butyldimethylsilyl chloride (1.524 g, 10.11 mmol) was added to 1-benzhydrylazetidin-3-ol (CAS no. 18621-17-5) (2.2 g, 9.19 mmol) and imidazole (1.565 g, 22.98 mmol) in DCM (46.0 mL) at r.t. under nitrogen. The resulting solution was stirred at r.t. for 3 hours. The reaction mixture was quenched with water, poured onto a phase separator and evaporated to afford the product (3.66 g, 113%). 1H NMR (400 MHz, CDCl3) δ 0.00 (6H, s), 0.85 (9H, s), 2.81 (2H, s), 3.52 (2H, s), 4.35 (1H, s), 4.40-4.49 (1H, m), 7.08-7.43 (10H, m); m/z (ES+) (M+H)+=354.55; HPLC tR=2.04 min.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08071585B2uspto-grants-2011_12